Ivd Jobs
Browse 10 exciting jobs hiring in Ivd now. Check out companies hiring such as Illumina, Awesome Motive, Cellanome in San Antonio, Irving, Grand Rapids.
As a Validation Engineer 2 at Illumina's San Diego site, you will lead validation strategy, execute IQ/OQ/PQ and testing activities, and ensure compliance with regulatory and quality standards for manufacturing processes and systems.
ARK Diagnostics is hiring a Regulatory Affairs Specialist II to own international product registrations, support submissions (e.g., 510(k), De Novo, IVDR), and maintain regulatory compliance at its Fremont, CA facility.
ARK Diagnostics is seeking an experienced Senior Clinical Affairs Specialist to lead clinical validation studies, specimen acquisition, and regulatory documentation for IVD assays at the Fremont, CA facility.
ARK Diagnostics is hiring a Regulatory Affairs Specialist II to manage international device registrations, prepare regulatory submissions (including 510(k), De Novo, and IVDR technical documentation), and support lifecycle compliance for IVD and medical device products.
Cellanome is hiring a Staff Technical Program Manager to lead cross-functional instrument development programs (hardware, software, assay, systems integration) and drive on-time delivery from concept through V&V in San Diego.
Veracyte is hiring a hands-on Clinical Trials Assistant in San Diego to manage sample logistics, clinical data entry, and operational support for ongoing clinical studies.
Lead physician engagement at RDI by creating momentum with clinicians and converting conversations into committed site participation for complex IVD and device studies.
LGC Clinical Diagnostics is hiring a Sales Support Specialist to support the End User Sales Team with customer triage, quote management, CRM updates and technical call routing.
Velsera is looking for a remote Manager, Technical Services to lead and scale clinical services teams, own customer success and QMS feedback processes, and translate client needs into operational and product improvements.
Lead and own multi-site diagnostic clinical studies at RDI, ensuring on-time sample collection, data quality, and clear sponsor communication in a fast-moving CRO environment.
